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A simple and sensitive resonance light scattering method based on aggregation of gold nanoparticles for selective detection of microRNA-21

机译:基于金纳米颗粒聚集的简单灵敏共振光散射方法,用于microRNA-21的选择性检测

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摘要

We describe a simple, sensitive and selective resonance light scattering (RLS) method based on analyte-induced aggregation of gold nanoparticles (GNs) for the determination of microRNAs (miRNAs). The RLS sensor is fabricated by modifying GNs with two strands of cDNA sequence, which can averagely complement the target miRNA. When the target miRNA is introduced, the cDNAs can complement the target miRNAs, thereby forming a cDNARNA heteroduplex. The formation of cDNA RNA heteroduplex led to the aggregation of GNs, which promotes RLS enhancement. A limit of detection of 2.21 pM and a liner range from 10 to 200 nM (R-2 = 0.9981) are achieved using this assay. Moreover, this strategy was further used for the determination of miRNAs in a human serum sample with satisfying results, offering a significant potential for clinical application.
机译:我们描述了一种简单,灵敏和选择性的共振光散射(RLS)方法,该方法基于分析物诱导的金纳米颗粒(GNs)聚集来确定microRNA(miRNA)。通过用两条cDNA序列修饰GN来制造RLS传感器,可以平均补充靶标miRNA。当引入靶标miRNA时,cDNA可以互补靶标miRNA,从而形成cDNA RNA异源双链体。 cDNA RNA异源双链体的形成导致GNs聚集,从而促进RLS增强。使用此测定法可达到2.21 pM的检测限和10到200 nM的线性范围(R-2 = 0.9981)。此外,该策略还用于测定人血清样品中的miRNA,结果令人满意,为临床应用提供了巨大潜力。

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